Surfaces and Interfaces, Год журнала: 2025, Номер unknown, С. 106298 - 106298
Опубликована: Март 1, 2025
Язык: Английский
Surfaces and Interfaces, Год журнала: 2025, Номер unknown, С. 106298 - 106298
Опубликована: Март 1, 2025
Язык: Английский
Applied Catalysis B Environment and Energy, Год журнала: 2024, Номер 345, С. 123705 - 123705
Опубликована: Янв. 6, 2024
Язык: Английский
Процитировано
37Journal of Colloid and Interface Science, Год журнала: 2024, Номер 664, С. 500 - 510
Опубликована: Март 11, 2024
Язык: Английский
Процитировано
21Inorganic Chemistry Frontiers, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
The well-designed catalyst structure can significantly enhance the efficiency of photocatalytic H 2 , O and degradation TC. This study offers novel insights into constructing a visible photothermal assisted reaction system.
Язык: Английский
Процитировано
2Nano Energy, Год журнала: 2024, Номер 124, С. 109495 - 109495
Опубликована: Март 12, 2024
Язык: Английский
Процитировано
14Small, Год журнала: 2024, Номер 20(33)
Опубликована: Март 29, 2024
Designing a reasonable heterojunction is an efficient path to improve the separation of photogenerated charges and enhance photocatalytic activity. In this study, Cu
Язык: Английский
Процитировано
13Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(48)
Опубликована: Июль 31, 2024
Abstract Electrochemical sulfion oxidation reaction (SOR) offers a sustainable strategy for sulfion‐rich wastewater treatment, which can couple with cathodic hydrogen evolution (HER) energy‐saving production. However, the corrosion and passivation of sulfur species render inferior catalytic SOR performance, product, polysulfide, requires further acidification to recover cheap elementary sulfur. Here, we reported an amorphous high‐entropy sulfide catalyst CuCoNiMnCrS x nanosheets in situ growth on nickel foam (CuCoNiMnCrS /NF) SOR, achieved ultra‐low potential 0.25 V afford 100 mA cm −2 , stable electrolysis at as high 1 A h. These were endowed by manipulated chemical environments surrounding Cu + sites constructed “soft‐acid” “hard‐acid” adsorption/desorption sites, enabling synergistically boosted process during SOR. Moreover, developed electrochemical‐chemical tandem convert sulfions value‐added thiosulfate, providing good choice simultaneous utilization
Язык: Английский
Процитировано
11Chemosphere, Год журнала: 2024, Номер 359, С. 142316 - 142316
Опубликована: Май 10, 2024
Язык: Английский
Процитировано
10Journal of Photochemistry and Photobiology A Chemistry, Год журнала: 2025, Номер 462, С. 116275 - 116275
Опубликована: Янв. 15, 2025
Язык: Английский
Процитировано
1Carbon Capture Science & Technology, Год журнала: 2025, Номер unknown, С. 100377 - 100377
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
1Small, Год журнала: 2025, Номер unknown
Опубликована: Фев. 5, 2025
Abstract Achieving synergistic oxidation and reduction represents a significant challenge in the field of photocatalysis. In this study, hydrothermal/in situ construction Bi atom clusters within 2 Sn O 7 /ZnIn S 4 (BSO/ZIS) heterostructures is reported. These exhibit self‐accelerating charge‐transfer mechanisms facilitated by internal electric fields bonding bridges, resulting highly efficient light absorption capabilities. X‐ray photoelectron spectroscopy (XPS) Kelvin probe force microscopy (KPFM), as well theoretical calculations, indicate that canonical induction promotion electrons holes lowers activation energy CHO* generation, allowing simultaneous CO toluene over catalyst, enhances proton‐coupling electron‐transfer processes, unique reaction mechanism. The reactant, Bi‐Bi (B‐BSO/ZIS) heterostructure achieves rate to 726.3 µmol g −1 h (99.9% selectivity) benzaldehyde 2362.0 (98.0% selectivity), which increases activity 14.6 5.7 times compared pristine ZnIn . This study underscores significance modulating photocatalytic pathway through strategic selection metal reactants, contributing rational design photocatalysts for enhanced adsorption stabilization *H.
Язык: Английский
Процитировано
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